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CUCURBITACIN I

CAS No.
2222-07-3
Chemical Name:
CUCURBITACIN I
Synonyms
JSI-124;Ibamarin;ELATERIN B;NSC 521777;ELATERICIN B;CUCURBITACIN I;5-tetrahydroxy-;cucurbitacine(i);CUCURBITACIN I(SH);CUCURBITACIN I hplc
CBNumber:
CB6480840
Molecular Formula:
C30H42O7
Molecular Weight:
514.65
MDL Number:
MFCD09971044
MOL File:
2222-07-3.mol
MSDS File:
SDS
Last updated:2023-06-30 15:45:59

CUCURBITACIN I Properties

Melting point 148-150°C
Boiling point 698.3±55.0 °C(Predicted)
Density 1.26±0.1 g/cm3(Predicted)
storage temp. -20°C
solubility ≥22.45 mg/mL in DMSO; insoluble in EtOH; ≥51.2 mg/mL in H2O with ultrasonic
pka 8.51±0.70(Predicted)
form solid
color white to off-white
LogP 2.330 (est)
FDA UNII SHQ47990PH

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS06
Signal word  Danger
Hazard statements  H301
Precautionary statements  P301+P330+P331+P310
Hazard Codes  Xi,T+
Risk Statements  25-28
Safety Statements  1-22-45-36/37-28
RIDADR  UN 2811 6.1/PG 1
WGK Germany  3
RTECS  RC6200000
Toxicity LD50 oral in mouse: 5mg/kg
NFPA 704
0
2 0

CUCURBITACIN I price More Price(29)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich PHL89464 Cucurbitacin I phyproof? Reference Substance 2222-07-3 10MG $598 2024-03-01 Buy
Sigma-Aldrich C4493 Cucurbitacin I hydrate ≥95% (HPLC), solid 2222-07-3 1mg $153 2024-03-01 Buy
Sigma-Aldrich 238590 Cucurbitacin I, Cucumis sativus L. A cell-permeable and irreversible bitter triterpenoid compound (NCI identifier: NSC 521777) that displays anti-proliferative and antitumor properties both in vitro and in vivo. 2222-07-3 1MG $289 2024-03-01 Buy
Cayman Chemical 14747 Cucurbitacin I ≥98% 2222-07-3 1mg $96 2024-03-01 Buy
Cayman Chemical 14747 Cucurbitacin I ≥98% 2222-07-3 5mg $238 2024-03-01 Buy
Product number Packaging Price Buy
PHL89464 10MG $598 Buy
C4493 1mg $153 Buy
238590 1MG $289 Buy
14747 1mg $96 Buy
14747 5mg $238 Buy

CUCURBITACIN I Chemical Properties,Uses,Production

Uses

Cucurbitacin I can be useful in the study of edible vitalmelon fruit extract and adipogenesis.

Definition

ChEBI: A cucurbitacin that is 9,10,14-trimethyl-4,9-cyclo-9,10-secocholesta-2,5,23-triene substituted by hydroxy groups at positions 2, 16, 20 and 25 and oxo groups at positions 1, 11 and 22.

Biological Activity

Selective inhibitor of STAT3/JAK2 signaling. Inhibits the activation of STAT3 and JAK2 and displays no activity on Src, Akt, ERK and JNK. Suppresses phosphotyrosine levels of STAT3, inhibits STAT3 DNA binding and STAT3-mediated gene expression. Induces apoptosis in cell lines expressing constitutively active tyrosine-phosphorylated STAT3.

Biochem/physiol Actions

Cucurbitacin I (JSI-124) is a novel selective inhibitor of the janus kinase 2/signal transducer and activator of transcription 3 (JAK2/STAT3) signaling pathway with anti-proliferative and anti-tumor properties.

storage

Store at -20°C

References

blaskovich ma, sun j, cantor a et al. discovery of jsi-124 (cucurbitacin i), a selective janus kinase/signal transducer and activator of transcription 3 signaling pathway inhibitor with potent antitumor activity against human and murine cancer cells in mice.cancer res. 2003 mar 15;63(6):1270-9.yu h, lee h, herrmann a et al. revisiting stat3 signalling in cancer: new and unexpected biological functions.nat rev cancer. 2014 nov;14(11):736-46. doi: 10.1038/nrc3818.song j, liu h, li z et al. cucurbitacin i inhibits cell migration and invasion and enhances chemosensitivity in colon cancer. oncol rep. 2015 apr;33(4):1867-71. qi j, xia g, huang cr et al. jsi-124 (cucurbitacin i) inhibits tumor angiogenesis of human breast cancer through reduction of stat3 phosphorylation. am j chin med. 2015;43(2):337-47.kim hj, kim jk et al. antiangiogenic effects of cucurbitacin-i. arch pharm res. 2015 feb;38(2):290-8. yuan g, yan sf, xue h et al. cucurbitacin i induces protective autophagy in glioblastoma in vitro and in vivo. j biol chem. 2014 apr 11;289(15):10607-19.

CUCURBITACIN I Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 112)Suppliers
Supplier Tel Email Country ProdList Advantage
Shanghai Zheyan Biotech Co., Ltd.
18017610038 zheyansh@163.com CHINA 3620 58
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
Chengdu Biopurify Phytochemicals Ltd.
+8618080483897 sales@biopurify.com China 3424 58
Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28180 58
Shaanxi Pioneer Biotech Co., Ltd .
+8613259417953 sales@pioneerbiotech.com China 3000 58
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873 sales@chemdad.com China 39916 58
Aktin Chemicals, Inc.
028-85159085 info@aktinchem.com CHINA 1025 58
LEAPCHEM CO., LTD.
+86-852-30606658 market18@leapchem.com China 43348 58
Aladdin Scientific
+1-833-552-7181 sales@aladdinsci.com United States 52927 58
Jiaozuo Furuitang Pharmaceutical Co., Ltd. jzfrtcw@163.com China 8 58

View Lastest Price from CUCURBITACIN I manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
CUCURBITACIN I pictures 2019-07-06 CUCURBITACIN I
2222-07-3
US $1.00 / KG 1G 98% 100KG Career Henan Chemical Co
ELATERICIN B ELATERIN B CUCURBITACIN I WITH HPLC Cucurbitacin I hydrate Elatericin B, JSI-124, NSC 521777, 2,16α,20,25-Tetrahydroxy-9-methyl-19-Nor-9β,10α-lanosta-1,5,23-triene-3,11,22-trione (9β,10α,23E)-2,16α,20,25-Tetrahydroxy-9-methyl-19-norlanosta-1,5,23-triene-3,11,22-trione Ibamarin 2,16a,20,25-Tetrahydroxy-9b-methyl-10a-19-norlanosta-1,5,23(E)-triene-3,11,22-trione 2,16α,20,25-tetrahydroxy-9β-methyl-10α-19-norlanosta-1,5,23(E)-triene-3,11,22-trione 19-Norlanosta-1,5,23-triene-3,11,22-trione, 2,16,20,25-tetrahydroxy-9-methyl-, (9b,10a,16a,23E)- CUCURBITACIN I(SH) CUCURBITACIN I hplc (9β,10α,16α,23E)-2,16,20,25-Tetrahydroxy-9-methyl-19-norlanosta-1,5,23-triene-3,11,22-trione 2,16α,20,25-tetrahydroxy-9-methyl-19-Nor-9β,10α-lanosta-1,5,23-triene-3,11,22-trione NSC 521777 Cucurbitacin I (JSI-124) calebassine/cucurbitacin CUCURBITACIN I 1,2-dehydroelatericina 19-nor-9-beta,10-alpha-lanosta-1,5,23-triene-3,11,22-trione,9-methyl-2,16,20,2 JSI-124 2,16alpha,20,25-tetrahydroxy-9beta-methyl-10alpha-19-norlanosta-1,5,23(E)-triene-3,11,22-trione 5-tetrahydroxy- cucurbitacine(i) Cucurbitacin I (Elatericin B 19-Norlanosta-1,5,23-triene-3,11,22-trione, 2,16,20,25-tetrahydroxy-9-methyl-, (9β,10α,16α,23E)- 2222-07-3 2222-7-3 Inhibitor Herb extract API Tri-Terpenoids